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Structure of 43088-42-2
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Ethyl 2-amino-4-methylthiophene-3-carboxylate features a thiophene core with complementary amino and methylthio functionalities, enabling direct incorporation into heterocyclic scaffolds. This bench-stable reagent facilitates efficient access to biologically relevant thienyl derivatives under standard conditions.
Ethyl 2-amino-4-methylthiophene-3-carboxylate serves as a versatile heterocyclic building block for medicinal chemistry and agrochemical synthesis. Its amino and ester functionalities enable straightforward derivatization via amidation, acylation, and coupling reactions. The methylthio group offers a handle for selective oxidation or displacement, while the thiophene core provides structural rigidity and π-conjugation beneficial in target-oriented synthesis. Bench-stable and readily purified by column chromatography, it functions effectively in standard reaction protocols.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362+P364
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Lot numbers can be found on the outside label of a product: